Department of Medical Oncology, CHU la Timone, AP-HM, Marseille, France.
Department of Medical Oncology, Hôpital Saint-André, Bordeaux University Hospital-CHU, Bordeaux, France.
Cancer Med. 2021 Jun;10(12):3952-3963. doi: 10.1002/cam4.3953. Epub 2021 May 25.
Prognosis of recurrent or metastatic (R/M) head and neck squamous cell carcinoma (HNSCC) remains poor. The addition of cetuximab, to platinum and fluorouracil chemotherapy (EXTREME regimen) has been shown to improve patients' outcomes in first-line settings.
We conducted a retrospective, multicenter study, including HNSCC that progressed after a first line of platinum-based chemotherapy and cetuximab, treated either by paclitaxel + cetuximab (PC) or paclitaxel alone (P), between January 2010 and April 2018. The end points were overall survival (OS), progression-free survival (PFS), and overall response rates (ORR). Patients were matched according to their propensity scores, estimated with a logistic regression model. The secondary objectives were to study the safety profile and to look for prognostic and predictive factors of effectiveness.
Of the 340 identified patients, 262 were included in the analysis, 165 received PC, and 97 received P. In unmatched population, ORR was 16.4% with PC and 6.2% for P. Median PFS was 2.9 months [95% Confidence Interval 2.7-3.0] for PC versus 2.5 months [2.2-2.7] for P, hazard ratio (HR) = 0.770 [0.596-0.996]. Median OS was 5.5 months [4.4-6.9] for PC versus 4.2 months [3.4-4.8] for P, HR = 0.774 [0.590-1.015]. In multivariate analysis, PC was associated with better PFS and OS. These results were consistent in matched-paired population. Previous cetuximab maintenance for more than 3 months was predictive of better OS with PC.
Although the continuation of cetuximab in combination with paclitaxel after EXTREME provides moderate benefit, it could be an interesting option for selected patients.
复发性或转移性(R/M)头颈部鳞状细胞癌(HNSCC)的预后仍然很差。在一线治疗中,顺铂和氟尿嘧啶化疗(EXTREME 方案)中加入西妥昔单抗已被证明可以改善患者的预后。
我们进行了一项回顾性、多中心研究,纳入了 2010 年 1 月至 2018 年 4 月期间接受过一线基于铂类化疗和西妥昔单抗治疗、随后接受紫杉醇+西妥昔单抗(PC)或紫杉醇单药(P)治疗的 HNSCC 患者。主要终点为总生存期(OS)、无进展生存期(PFS)和总缓解率(ORR)。根据逻辑回归模型估计的倾向评分对患者进行匹配。次要目标是研究安全性概况,并寻找有效性的预后和预测因素。
在确定的 340 名患者中,有 262 名患者纳入分析,其中 165 名接受了 PC 治疗,97 名接受了 P 治疗。在未匹配的人群中,PC 的 ORR 为 16.4%,P 为 6.2%。PC 的中位 PFS 为 2.9 个月[95%置信区间 2.7-3.0],P 为 2.5 个月[2.2-2.7],风险比(HR)=0.770[0.596-0.996]。PC 的中位 OS 为 5.5 个月[4.4-6.9],P 为 4.2 个月[3.4-4.8],HR=0.774[0.590-1.015]。多变量分析显示,PC 与更好的 PFS 和 OS 相关。在匹配的配对人群中,这些结果是一致的。以前接受西妥昔单抗维持治疗超过 3 个月与 PC 的更好 OS 相关。
尽管 EXTREME 后继续使用西妥昔单抗联合紫杉醇可以带来适度的获益,但对于某些患者来说,这可能是一个有趣的选择。